Skip to main content

Featured post

🧠 Steps in ICSR (Individual Case Safety Report) – A Complete Journey of Ensuring Patient Safety

Wipro Hiring: Case Processing Associates (Pharmacovigilance)

 

Wipro Hiring: Case Processing Associates (Pharmacovigilance) – Pune

Wipro is Hiring: Case Processing Associates (Pharmacovigilance) – Pune

Wipro is inviting applications from Pharmacy, Nursing, and Life Science graduates for Case Processing Associate roles in Pharmacovigilance (PV).


Role Highlights

  • Job Title: Case Processing Associate (Pharmacovigilance)
  • Location: Pune
  • Work Mode: Onsite (Work From Office)
  • Shifts: General / Rotational
  • Eligibility: B.Pharm / Nursing / BDS / BMS / Life Sciences
  • Experience: Freshers to 4 years

Who Can Apply

This role is ideal for candidates who:

  • Hold a degree in B.Pharm, Nursing, BDS, BMS, or Life Sciences
  • Are freshers or have up to 4 years of relevant experience
  • Are comfortable with onsite work and general/rotational shifts 

Key Responsibilities (Typical for PV Case Processing)

  • Collect, review, and process individual case safety reports (ICSRs)
  • Ensure completeness, accuracy, and compliance with PV guidelines
  • Perform data entry and medical coding in safety databases
  • Support case narrative writing and follow-up activities
  • Collaborate with cross-functional teams to meet timelines and quality metrics

Note: Responsibilities listed are typical for PV roles and may vary by project.

How to Apply

Send your updated resume to: soniya.soniya@wipro.com

Subject line suggestion: “Application – Case Processing Associate (PV) – Pune – [Your Name]”

Tips to Boost Your Shortlisting

  • Highlight PV coursework, internships, or pharmacology projects
  • Mention familiarity with MedDRA coding, ICH-GCP, and safety databases (if applicable)
  • Show flexibility for rotational shifts and onsite work

Why Consider Pharmacovigilance at Wipro?

  • Opportunity to work on large-scale global PV processes
  • Structured training and process-driven environment
  • Good entry point for fresh graduates entering drug safety

FAQs

Is this role open to freshers?

Yes. Candidates from freshers to 4 years of experience are eligible.

Is this work from home?

No. The role is onsite in Pune.

What degrees are eligible?

B.Pharm, Nursing, BDS, BMS, and Life Sciences graduates are eligible.

How do I apply?

Email your resume to soniya.soniya@wipro.com.


Disclaimer: This post is for informational purposes. For the most accurate and updated details, please reach out to Wipro via the email provided or check the official careers page.

Comments

Popular posts from this blog

Top Pharmacovigilance Interview Questions and Answers (Fresher to Experience)

Title: Pharmacovigilance Interview Questions and Answers Define Pharmacovigilance Pharmacovigilance is the science of collecting, monitoring, researching, evaluating, and interpreting data from healthcare professionals and patients about the adverse effects of medicines, biological products, herbal treatments, and other medical substances. The purpose is to ensure drug safety and protect public health. What Are the Minimum Criteria Required for a Valid Case? A valid safety case must contain: • An identifiable reporter • An identifiable patient • A suspect product • An adverse drug event Define Adverse Drug Event (ADE) An Adverse Drug Event is any undesirable medical occurrence that happens after the administration of a pharmaceutical product, regardless of whether it is related to the drug. Define Adverse Drug Reaction (ADR) An Adverse Drug Reaction is a harmful, unintended response to a drug that occurs at normal doses used for diagnosis, treatment, or prevention of...

Clinical Research Associate (CRA) Jobs – CBCC Global Research | Delhi, Bengaluru, Pune, Kolkata

CBCC Global Research is hiring experienced and enthusiastic Clinical Research Associates (CRAs) to support innovative oncology and non-oncology clinical studies across India. Locations Delhi • Bengaluru • Pune • Kolkata What You’ll Bring 1–4 years of on-site monitoring experience in clinical trials Strong understanding of GCP , ICH guidelines , and regulatory processes Excellent communication and organizational skills Willingness to travel for site monitoring visits Why Join CBCC Global Research Work on cutting-edge oncology and non-oncology studies Collaborative, growth-oriented environment Competitive compensation with strong learning opportunities How to Apply Send your updated CV to sonu.gupta@cbcc.global with the subject line: Application – CRA – [Your Name] – [Preferred City] About CBCC Global Research CBCC Global Research partners with leading investigators and institutions to deliver high-quality clinical research with patient-centric...